Congenital long QT syndrome of particularly malignant course connected with so far unknown mutation in the sodium channel SCN5A gene

التفاصيل البيبلوغرافية
العنوان: Congenital long QT syndrome of particularly malignant course connected with so far unknown mutation in the sodium channel SCN5A gene
المؤلفون: Uziębło-Życzkowska, Beata, Michałkiewicz, Dariusz, Jackun-Podleśna, Anna, Gielerak, Grzegorz, Zienciuk-Krajka, Agnieszka
المصدر: Cardiology Journal; Vol 20, No 1 (2013); 78-82
بيانات النشر: Via Medica
سنة النشر: 2013
المجموعة: Via Medica Journals
مصطلحات موضوعية: long QT syndrome, sudden cardiac arrest, new mutation gene SCN5A in LQTS
الوصف: This article presents the case of a 35 year-old male with long QT syndrome (LQTS) who suffered from sudden cardiac arrest. Even though asymptomatic LQTS had been diagnosed, the patient had not undergone any medical treatment. His two daughters, aged four and seven, were also diagnosed with LQTS. A new, previously unknown, mutation of the SCN5A gene has been found in the family. The older daughter died suddenly before implantable cardioverterdefibrillator (ICD) implantation, but the father and the younger daughter have been implanted with ICDs.
نوع الوثيقة: other/unknown material
وصف الملف: application/pdf; application/xhtml+xml
اللغة: unknown
العلاقة: https://journals.viamedica.pl/cardiology_journal/article/view/CJ.2013.0012Test
DOI: 10.5603/CJ.2013.0012
الإتاحة: https://doi.org/10.5603/CJ.2013.0012Test
https://journals.viamedica.pl/cardiology_journal/article/view/CJ.2013.0012Test
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رقم الانضمام: edsbas.3C31A0F8
قاعدة البيانات: BASE